EP2157048B1 - Reformer and indirect internal reforming-type high-temperature fuel cell - Google Patents

Reformer and indirect internal reforming-type high-temperature fuel cell Download PDF

Info

Publication number
EP2157048B1
EP2157048B1 EP08752801.4A EP08752801A EP2157048B1 EP 2157048 B1 EP2157048 B1 EP 2157048B1 EP 08752801 A EP08752801 A EP 08752801A EP 2157048 B1 EP2157048 B1 EP 2157048B1
Authority
EP
European Patent Office
Prior art keywords
reformer
reforming
fuel cell
high temperature
temperature fuel
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Not-in-force
Application number
EP08752801.4A
Other languages
German (de)
French (fr)
Other versions
EP2157048A4 (en
EP2157048A1 (en
Inventor
Susumu Hatada
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eneos Corp
Original Assignee
Nippon Oil Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Oil Corp filed Critical Nippon Oil Corp
Publication of EP2157048A1 publication Critical patent/EP2157048A1/en
Publication of EP2157048A4 publication Critical patent/EP2157048A4/en
Application granted granted Critical
Publication of EP2157048B1 publication Critical patent/EP2157048B1/en
Not-in-force legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/06Combination of fuel cells with means for production of reactants or for treatment of residues
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/008Details of the reactor or of the particulate material; Processes to increase or to retard the rate of reaction
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/0207Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds the fluid flow within the bed being predominantly horizontal
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J8/00Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes
    • B01J8/02Chemical or physical processes in general, conducted in the presence of fluids and solid particles; Apparatus for such processes with stationary particles, e.g. in fixed beds
    • B01J8/0285Heating or cooling the reactor
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • C01B3/38Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • C01B3/38Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
    • C01B3/382Multi-step processes
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B3/00Hydrogen; Gaseous mixtures containing hydrogen; Separation of hydrogen from mixtures containing it; Purification of hydrogen
    • C01B3/02Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen
    • C01B3/32Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air
    • C01B3/34Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents
    • C01B3/38Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts
    • C01B3/384Production of hydrogen or of gaseous mixtures containing a substantial proportion of hydrogen by reaction of gaseous or liquid organic compounds with gasifying agents, e.g. water, carbon dioxide, air by reaction of hydrocarbons with gasifying agents using catalysts the catalyst being continuously externally heated
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B6/00Hydrides of metals including fully or partially hydrided metals, alloys or intermetallic compounds ; Compounds containing at least one metal-hydrogen bond, e.g. (GeH3)2S, SiH GeH; Monoborane or diborane; Addition complexes thereof
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/06Combination of fuel cells with means for production of reactants or for treatment of residues
    • H01M8/0606Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants
    • H01M8/0612Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material
    • H01M8/0625Combination of fuel cells with means for production of reactants or for treatment of residues with means for production of gaseous reactants from carbon-containing material in a modular combined reactor/fuel cell structure
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/10Fuel cells with solid electrolytes
    • H01M8/12Fuel cells with solid electrolytes operating at high temperature, e.g. with stabilised ZrO2 electrolyte
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00389Controlling the temperature using electric heating or cooling elements
    • B01J2208/00407Controlling the temperature using electric heating or cooling elements outside the reactor bed
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/00008Controlling the process
    • B01J2208/00017Controlling the temperature
    • B01J2208/00389Controlling the temperature using electric heating or cooling elements
    • B01J2208/00415Controlling the temperature using electric heating or cooling elements electric resistance heaters
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2208/00Processes carried out in the presence of solid particles; Reactors therefor
    • B01J2208/02Processes carried out in the presence of solid particles; Reactors therefor with stationary particles
    • B01J2208/021Processes carried out in the presence of solid particles; Reactors therefor with stationary particles comprising a plurality of beds with flow of reactants in parallel
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2219/00Chemical, physical or physico-chemical processes in general; Their relevant apparatus
    • B01J2219/19Details relating to the geometry of the reactor
    • B01J2219/192Details relating to the geometry of the reactor polygonal
    • B01J2219/1923Details relating to the geometry of the reactor polygonal square or square-derived
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/02Processes for making hydrogen or synthesis gas
    • C01B2203/0205Processes for making hydrogen or synthesis gas containing a reforming step
    • C01B2203/0227Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step
    • C01B2203/0233Processes for making hydrogen or synthesis gas containing a reforming step containing a catalytic reforming step the reforming step being a steam reforming step
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/06Integration with other chemical processes
    • C01B2203/066Integration with other chemical processes with fuel cells
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/08Methods of heating or cooling
    • C01B2203/0805Methods of heating the process for making hydrogen or synthesis gas
    • C01B2203/0811Methods of heating the process for making hydrogen or synthesis gas by combustion of fuel
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/08Methods of heating or cooling
    • C01B2203/0805Methods of heating the process for making hydrogen or synthesis gas
    • C01B2203/085Methods of heating the process for making hydrogen or synthesis gas by electric heating
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/10Catalysts for performing the hydrogen forming reactions
    • C01B2203/1005Arrangement or shape of catalyst
    • C01B2203/1011Packed bed of catalytic structures, e.g. particles, packing elements
    • CCHEMISTRY; METALLURGY
    • C01INORGANIC CHEMISTRY
    • C01BNON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
    • C01B2203/00Integrated processes for the production of hydrogen or synthesis gas
    • C01B2203/12Feeding the process for making hydrogen or synthesis gas
    • C01B2203/1205Composition of the feed
    • C01B2203/1211Organic compounds or organic mixtures used in the process for making hydrogen or synthesis gas
    • C01B2203/1235Hydrocarbons
    • C01B2203/1247Higher hydrocarbons
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01MPROCESSES OR MEANS, e.g. BATTERIES, FOR THE DIRECT CONVERSION OF CHEMICAL ENERGY INTO ELECTRICAL ENERGY
    • H01M8/00Fuel cells; Manufacture thereof
    • H01M8/10Fuel cells with solid electrolytes
    • H01M8/12Fuel cells with solid electrolytes operating at high temperature, e.g. with stabilised ZrO2 electrolyte
    • H01M2008/1293Fuel cells with solid oxide electrolytes
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E60/00Enabling technologies; Technologies with a potential or indirect contribution to GHG emissions mitigation
    • Y02E60/30Hydrogen technology
    • Y02E60/50Fuel cells

Definitions

  • the present invention relates to a reformer that reforms a hydrocarbon-based fuel, such as kerosene, to produce a hydrogen-containing gas and an indirect internal reforming high temperature fuel cell that generates electric power using the hydrogen-containing gas produced by the reformer.
  • a reformer that reforms a hydrocarbon-based fuel, such as kerosene, to produce a hydrogen-containing gas and an indirect internal reforming high temperature fuel cell that generates electric power using the hydrogen-containing gas produced by the reformer.
  • a solid oxide fuel cell (sometimes abbreviated as SOFC hereinafter) is supplied with a hydrogen-containing gas (reformed gas) produced by reforming a hydrocarbon-based fuel, such as kerosene and city gas, at a reformer.
  • SOFC hydrogen-containing gas
  • the SOFC generates electric power by electrochemical reaction of the reformed gas and air.
  • the SOFC typically operates at a high temperature approximately ranging from 550°C to 1000°C.
  • reforming reaction there are various types of reforming reaction, such as steam reforming and partial oxidation reforming.
  • the steam reforming is most commonly used because the reformed gas produced by the steam reforming contains a high concentration of hydrogen.
  • the steam reforming is an extremely highly endothermic reaction and requires a relatively high reaction temperature of about 550°C to 750°C and therefore a high temperature heat source. Therefore, an indirect internal reforming SOFC has been developed that is provided with a reformer disposed in the vicinity of the SOFC (at a location where the reformer receives thermal radiation from the SOFC) so that the reformer is heated by the radiation heat from the SOFC.
  • an indirect internal reforming SOFC burns the anode off gas containing a combustible component (gas discharged from the anode of the SOFC) in a container (module container) of the indirect internal reforming SOFC and uses the combustion heat as a heat source to heat the reformer (Patent Document 1).
  • Reforming catalysts having various kinds of structure such as a granular catalyst (Patent Document 2) and honeycomb-type catalysts (Patent Documents 3 and 4), are known.
  • the granular catalyst is relatively inexpensive and widely used.
  • a granular catalyst bed has a low effective thermal conductivity. If the granular bed has a large height in the direction of the thermal radiation from the SOFC, a large temperature difference can occur in the direction, resulting in an insufficient reforming reaction in a part at a lower temperature. In this case, a larger amount of catalyst is required, and thus, the reformer has to have a larger size.
  • the local temperature decrease may be prevented by turning back the flow of the reforming gas as described in Patent Document 2. However, if the flow of the gas is turned back in order to uniform the heat distribution in the reformer, the cross sectional area of the flow channel decreases, or the length of the flow channel increases. This causes increase in the pressure loss and in the required power and the size of an auxiliary machine, such as a blower for supplying gas to the reformer.
  • An object of the present invention is to provide a reformer that uses a relatively inexpensive granular catalyst and can provide a more uniform temperature distribution in a catalyst bed while suppressing increase in the size of the reformer, the pressure loss, and the required power and size of an auxiliary machine.
  • An another object of the present invention is to provide a more compact indirect internal reforming high temperature fuel cell that has such a reformer while suppressing increase in cost.
  • the present invention provides an indirect internal reforming high temperature fuel cell as claimed in claim 1.
  • the present invention provides a reformer that uses a relatively inexpensive granular catalyst and can provide a more uniform temperature distribution in a catalyst bed while suppressing increase in the size of the reformer, the pressure loss, and the required power and size of an auxiliary machine.
  • the present invention provides a more compact indirect internal reforming high temperature fuel cell that has such a reformer while suppressing increase in cost.
  • FIG. 1 is a schematic cross-sectional side view of an indirect internal reforming SOFC, which is an example of an indirect internal reforming high temperature fuel cell according to the present invention.
  • This drawing shows a cross section perpendicular to the direction of flow of a gas in a reformer (the direction of flow of a reformed gas).
  • the reformed gas flows in the direction perpendicular to the sheet of the drawing.
  • the indirect internal reforming SOFC has a reformer 1 that produces a hydrogen-containing gas (reformed gas) from a hydrocarbon-based fuel using a steam reforming reaction and an SOFC 6 that generates electric power using the hydrogen-containing gas.
  • the hydrogen-containing gas (reformed gas) produced by the reformer 1 is supplied to an anode of the SOFC 6, an oxygen-containing gas, such as air, is supplied to a cathode of the SOFC 6, and the SOFC generates electric power by an electrochemical reaction between hydrogen and oxygen.
  • the indirect internal reforming SOFC further has a housing 7 (sometimes referred to as a module container hereinafter) that houses the reformer and the SOFC. That is, the reformer and the SOFC are modularized.
  • the reformer 1 has a reactor vessel (referred to also as a reforming vessel hereinafter) 2 and a reforming catalyst bed 5 packed with a granular catalyst housed in the reactor vessel 2.
  • the reforming catalyst has steam reforming activity.
  • the reformer 1 is disposed at a position where the reformer 1 receives thermal radiation from the SOFC 6.
  • the reformer has the shape of a rectangular parallelepiped.
  • the SOFC also has the shape of a rectangular parallelepiped.
  • the reformer is disposed above the SOFC. At least in rated operation, the reforming vessel is heated at the lower surface by radiation heat from the SOFC. As an anode off gas (gas discharged from the anode) is burned on the upper surface of the SOFC, the reforming vessel is heated at the lower surface also by the combustion heat.
  • the reformer has a partition plate 3 that divides the reforming catalyst bed into at least two sections.
  • the partition plate 3 extends in the reforming vessel from a part which is at a higher temperature in rated operation to a part which is at a lower temperature in rated operation.
  • the partition plate will be sometimes referred to as a first partition plate.
  • two planar partition plates 3 extend in the vertical direction. That is, the partition plates 3 extend from the surface (the lower surface) of the reforming vessel 2 facing the SOFC to the upper surface of the reforming vessel 2, the upper surface being located farther from the SOFC than the lower surface.
  • one planar partition plate 4 extending in the horizontal direction is provided in addition to the first partition plates.
  • the partition plate 4 is preferably used to provide a uniform heat distribution in lateral direction.
  • this partition plate will be sometimes referred to as a second partition plate.
  • the partition plates 3 and the partition plate 4 divide the reforming catalyst bed into six sections in total in the plane perpendicular to the direction of flow of the reforming gas.
  • the first partition plate has a thermal conductivity higher than the effective thermal conductivity of the reforming catalyst bed.
  • a thermal conductivity thereof is higher than the effective thermal conductivity of the reforming catalyst bed.
  • the effective thermal conductivity of the catalyst bed is an apparent thermal conductivity on the assumption that the catalyst bed is homogeneous and can be measured or calculated by an appropriate method.
  • the partition plates may be made of any appropriate material that is resistant to use environment and has a thermal conductivity higher than the effective thermal conductivity of the catalyst bed, such as stainless steel.
  • the partition plates are preferably made of the same material as the reactor vessel.
  • the reactor vessel of the reformer is formed of metal plates, and the metal plates have a thermal conductivity higher than the effective thermal conductivity of the catalyst bed
  • the first and second partition plates are preferably made of the same metal as the reforming vessel.
  • the shape of the partition plates is not limited to the planar shape but may be any appropriate shape, such as a shape of a bent plate.
  • first partition plates 3 are disposed at regular intervals to trisect the reforming catalyst bed in the horizontal direction.
  • the present invention is not limited to this configuration. It is essential only that the first partition plate(s) extends in the reforming vessel from a part heated to a higher temperature in rated operation toward a part heated to a lower temperature in rated operation. As a result, the partition plate(s) extends from a part closer to the heat source to a part farther from the heat source.
  • FIGS 2, 3 and 4 shows an example of a reformer that can replace the reformer shown in Figure 1 .
  • These drawings are also schematic cross-sectional views taken perpendicularly to the direction of flow of the gas in the reformer.
  • first partition plates 3 are disposed at higher densities in areas closer to the center (in the horizontal direction) of the reformer and at lower densities in areas farther from the center.
  • first partition plates 3 are disposed to radially extend from the center of the lower surface of the reformer vessel.
  • first partition plates 3 in the shape of a curved surface are disposed to radially extend from the center of the lower surface of the reformer vessel.
  • an appropriate one of the configurations shown in Figures 2, 3 and 4 may be selected.
  • the first partition plate is disposed not to inhibit the flow of the gas in the reformer.
  • the first partition plate may be disposed to extend along the direction of flow of the gas in the reformer (direction of flow of the reformed gas). The same holds true for the second partition plate.
  • the SOFC 6 heats the reactor vessel 2 from outside of the reactor vessel 2.
  • the present invention is not limited to this configuration. Even if the reformer is provided with any other heat source than the fuel cell and the reactor vessel is heated from outside by the heat source, the first partition plates provide the same effect.
  • the reformer may have combusting means, such as a burner and a catalyst combustor, and the reforming vessel may be heated from outside by the combusting means.
  • the reformer may have heating means, such as an electric heater, provided outside the reactor vessel, and the reforming vessel may be heated from outside by the heating means.
  • the reformer may be equipped with a heat source that heats the catalyst bed inside the reactor vessel.
  • Figure 5 shows an indirect internal reforming high temperature fuel cell in which a reformer 1 has a heating means, such as an electric heater 8, inside a reactor vessel 2, and a catalyst bed is heated inside the reactor vessel 2 by the heating means. Also in this case, the first partition plates provide the same effect.
  • the reformer according to the present invention has a partition plate made of a material, such as metal, having a thermal conductivity higher than the effective thermal conductivity of the catalyst bed.
  • the partition plate extends in the reactor vessel from a part which is at a higher temperature in rated operation to a part which is at a lower temperature in rated operation. Therefore, the thermal radiation from the high temperature fuel cell can be efficiently conducted to the entire catalyst bed, the catalyst bed can be more uniformly heated to a higher temperature, and the size of the reformer can be reduced.
  • hydrocarbon-based fuel selected from among compounds of which molecules contain carbon and hydrogen (may also contain other elements such as oxygen) or mixtures thereof that are well known as a feedstock for reformed gas in the field of the high temperature fuel cell.
  • compounds of which molecules contain carbon and hydrogen such as hydrocarbons and alcohols.
  • hydrocarbon fuels such as methane, ethane, propane, butane, natural gas, liquefied petroleum gas (LPG), city gas, gasoline, naphtha, kerosene and gas oil, alcohols such as methanol and ethanol, and ethers such as dimethyl ether may be used.
  • kerosene and LPG are preferred because they are readily available.
  • kerosene and LPG can be stored in a stand-alone manner and therefore are useful in areas where the city gas pipeline is not built.
  • high temperature fuel cells using kerosene or LPG are useful as an emergency power supply.
  • Kerosene is particularly preferred because it is easy to handle.
  • the present invention may be suitably applied to an indirect internal reforming fuel cell in which a reformer can be heated by thermal radiation from a high temperature fuel cell.
  • a molten carbonate fuel cell MCFC
  • MCFC molten carbonate fuel cell
  • the SOFC may be selected, as appropriate, from well-known SOFCs having various shapes, such as planar SOFCs and tubular SOFCs.
  • the SOFC may have an appropriate shape, such as a rectangular parallelepiped stack of planar SOFCs (including a cubic stack of planar SOFCs), a cylindrical SOFC stack, a bundle of tubular SOFC cells, and a cylindrical tubular SOFC cells.
  • Typical electrolytes used in the SOFC include oxygen-ion conductive ceramic and proton-ion conductive ceramic.
  • the MCFC may also be appropriately selected from among well-known MCFCs.
  • the SOFC and MCFC may be a single cell. However, in practice, a stack or bundle in which a plurality of single cells is arrayed is preferably used. In that case, the number of stacks or bundles can be one or more.
  • the reformer has a reforming catalyst bed packed with a granular catalyst having steam reforming activity in a reactor vessel.
  • the reforming catalyst having steam reforming activity may be selected, as appropriate, from among steam reforming catalysts which have steam reforming activity and autothermal reforming catalysts which have both of partial oxidation reforming activity and steam reforming activity.
  • the hydrocarbon-based fuel vaporized beforehand as required
  • steam and if necessary an oxygen-containing gas, such as air may be supplied each independently or mixed beforehand to the reformer (reforming catalyst bed).
  • the reforming gas is supplied to the anode of the high temperature fuel cell.
  • the indirect internal reforming SOFC has a reformer that produces a reforming gas containing hydrogen from a hydrocarbon-based fuel by a steam reforming reaction and a SOFC.
  • the reformer may perform a steam reforming reaction or perform autothermal reforming in which the steam reforming reaction is accompanied with the partial oxidation reaction. From the viewpoint of power generation efficiency of the SOFC, it is preferred that no partial oxidation reaction occurs.
  • the autothermal reforming is designed so that the steam reforming is predominant, and therefore, the overall reforming reaction is endothermic.
  • the heat required for the reforming reaction is supplied from the SOFC.
  • the reformer and the SOFC are housed in one module container and modularized.
  • the reformer is disposed at a position where the reformer receives the thermal radiation from the SOFC. This arrangement allows the reformer to be heated by the thermal radiation from the SOFC during electric power generation.
  • the anode off gas discharged from the SOFC may be burned at the outlet of the cell to heat the
  • the reformer is preferably disposed at a position where direct radiation heat transfer from the SOFC to the outer surface of the reformer is possible. Therefore, it is preferred that there is substantially no obstacle between the reformer and the SOFC, or in other words, it is preferred to make the region between the reformer and the SOFC be an empty space. In addition, the distance between the reformer and the SOFC is preferably as short as possible.
  • Each supply gas is appropriately heated as required before being supplied to the reformer or the SOFC.
  • the module container may be any appropriate container capable of housing the SOFC and the reformer.
  • the module container may be made of any appropriate material having resistance to the environment in which the module container is used, such as stainless steel. Connection ports are provided for the module container for gas interfacing or the like as required.
  • the module container is preferably hermetic in order to prevent communication between the interior of the module container and the surroundings (atmosphere).
  • Both the steam reforming catalyst and the autothermal reforming catalyst used in the reformer may be a well-known catalyst.
  • the steam reforming catalyst include a ruthenium-based catalyst or a nickel-based catalyst
  • examples of the autothermal reforming catalyst include a rhodium-based catalyst.
  • a granular catalyst is used.
  • the granular catalyst may be a catalyst formed by performing tablet compression, pulverization and then particle size selection within an appropriate range, a catalyst formed by extrusion molding, a catalyst formed by mixing with an appropriate binder and extrusion molding, or a powdered catalyst.
  • the catalyst may be a metal supported by a carrier formed by performing tablet compression, pulverization and then particle size selection within an appropriate range, a carrier formed by extrusion molding, a powdered carrier, or a carrier molded into an appropriate shape, such as a sphere, a ring, a tablet, a cylinder and a flake.
  • the reaction temperature of the steam reforming may range from 400°C to 1000°C, preferably from 500°C to 850°C, or more preferably from 550°C to 800°C.
  • the amount of steam introduced into the reaction system is defined as a ratio (steam/carbon ratio) of the number of moles of water molecules to the number of moles of carbon atoms contained in the hydrocarbon-based fuel, and the value of the ratio preferably falls within a range of 1 to 10, more preferably within a range of 1.5 to 7, or further preferably within a range of 2 to 5.
  • the space velocity (LHSV) is expressed as A/B, where A represents the flow rate (L/h) of the hydrocarbon-based fuel in the liquid state, and B represents the volume (L) of the catalyst bed.
  • the value of the LHSV is preferably set within a range of 0.05 to 20 h -1 , more preferably within a range of 0.1 to 10 h -1 , or further preferably within a range of 0.2 to 5 h -1 .
  • an oxygen-containing gas is added to the hydrocarbon-based fuel.
  • the oxygen-containing gas is preferably air because air is readily available, although the oxygen-containing gas may be pure oxygen.
  • the oxygen-containing gas may be added in order to balance the endothermic reaction involved with the steam reforming reaction and to obtain an amount of heat generation enough to keep or raise the temperature of the reforming catalyst bed and the SOFC.
  • the amount of oxygen-containing gas added is, as a ratio (oxygen/carbon ratio) of the number of moles of oxygen molecules to the number of moles of carbon atoms contained in the hydrocarbon-based fuel, preferably within a range of 0.005 to 1, more preferably within a range of 0.01 to 0.75, or further preferably within a range of 0.02 to 0.6.
  • the reaction temperature of the autothermal reforming reaction is set within a range of 400°C to 1000°C, preferably within a range of 450°C to 850°C, or more preferably within a range of 500°C to 800°C.
  • the space velocity (LHSV) is preferably selected within a range of 0.05 to 20, more preferably within a range of 0.1 to 10, or further preferably within a range of 0.2 to 5.
  • the amount of steam introduced into the reaction system is, as the steam/carbon ratio, preferably within a range of 1 to 10, more preferably within a range of 1.5 to 7, or further preferably within a range of 2 to 5.
  • the indirect internal reforming high temperature fuel cell according to the present invention may be additionally provided with a well-known component of a high temperature fuel cell system, as appropriate.
  • a component may be a desulfurizer that reduces the sulfur content of the hydrocarbon-based fuel; a vaporizer that vaporizes a liquid; pressure increasing means that pressurizes various kinds of fluids, such as a pump, a compressor and a blower; flow rate controlling means or flow path blocking/switching means that regulates the flow rate of a fluid or blocks a fluid flow or switches among fluid flow paths, such as a valve; a heat exchanger that performs heat exchange or heat recovery; a condenser that condenses a gas; heating/warming means that externally heats various kinds of equipment using steam or the like; storage means that stores the hydrocarbon-based fuel or a combustible material; an air or electric system for instrumentation; a signal system for control; a control device; and an electric system for output or powering.
  • the reformer and the indirect internal reforming high temperature fuel cell according to the present invention can be applied to, for example, a stationary or mobile power generating system or in a cogeneration system.

Description

    Technical Field
  • The present invention relates to a reformer that reforms a hydrocarbon-based fuel, such as kerosene, to produce a hydrogen-containing gas and an indirect internal reforming high temperature fuel cell that generates electric power using the hydrogen-containing gas produced by the reformer.
  • Background Art
  • Typically, a solid oxide fuel cell (sometimes abbreviated as SOFC hereinafter) is supplied with a hydrogen-containing gas (reformed gas) produced by reforming a hydrocarbon-based fuel, such as kerosene and city gas, at a reformer. The SOFC generates electric power by electrochemical reaction of the reformed gas and air. The SOFC typically operates at a high temperature approximately ranging from 550°C to 1000°C.
  • There are various types of reforming reaction, such as steam reforming and partial oxidation reforming. In particular, the steam reforming is most commonly used because the reformed gas produced by the steam reforming contains a high concentration of hydrogen. The steam reforming is an extremely highly endothermic reaction and requires a relatively high reaction temperature of about 550°C to 750°C and therefore a high temperature heat source. Therefore, an indirect internal reforming SOFC has been developed that is provided with a reformer disposed in the vicinity of the SOFC (at a location where the reformer receives thermal radiation from the SOFC) so that the reformer is heated by the radiation heat from the SOFC. In particular, an indirect internal reforming SOFC burns the anode off gas containing a combustible component (gas discharged from the anode of the SOFC) in a container (module container) of the indirect internal reforming SOFC and uses the combustion heat as a heat source to heat the reformer (Patent Document 1).
  • Reforming catalysts having various kinds of structure, such as a granular catalyst (Patent Document 2) and honeycomb-type catalysts (Patent Documents 3 and 4), are known. Among others, the granular catalyst is relatively inexpensive and widely used.
    • Patent Document 1: Japanese Patent Laid-Open No. 2004-319420
    • Patent Document 2: Japanese Patent Laid-Open No. H5-129026
    • Patent Document 3: Japanese Patent Laid-Open No. 2004-269332
    • Patent Document 4: Japanese Patent Laid-Open No. 2006-327904
    Disclosure of the Invention Problems to be Solved by the Invention
  • However, in general, a granular catalyst bed has a low effective thermal conductivity. If the granular bed has a large height in the direction of the thermal radiation from the SOFC, a large temperature difference can occur in the direction, resulting in an insufficient reforming reaction in a part at a lower temperature. In this case, a larger amount of catalyst is required, and thus, the reformer has to have a larger size. The local temperature decrease may be prevented by turning back the flow of the reforming gas as described in Patent Document 2. However, if the flow of the gas is turned back in order to uniform the heat distribution in the reformer, the cross sectional area of the flow channel decreases, or the length of the flow channel increases. This causes increase in the pressure loss and in the required power and the size of an auxiliary machine, such as a blower for supplying gas to the reformer.
  • An object of the present invention is to provide a reformer that uses a relatively inexpensive granular catalyst and can provide a more uniform temperature distribution in a catalyst bed while suppressing increase in the size of the reformer, the pressure loss, and the required power and size of an auxiliary machine.
  • An another object of the present invention is to provide a more compact indirect internal reforming high temperature fuel cell that has such a reformer while suppressing increase in cost.
  • Means for Solving the Problems
  • The present invention provides an indirect internal reforming high temperature fuel cell as claimed in claim 1.
  • Advantages of the Invention
  • The present invention provides a reformer that uses a relatively inexpensive granular catalyst and can provide a more uniform temperature distribution in a catalyst bed while suppressing increase in the size of the reformer, the pressure loss, and the required power and size of an auxiliary machine.
  • The present invention provides a more compact indirect internal reforming high temperature fuel cell that has such a reformer while suppressing increase in cost.
  • Brief Description of the Drawings
    • Figure 1 is a schematic cross-sectional side view for illustrating an example of an indirect internal reforming high temperature fuel cell according to the present invention;
    • Figure 2 is a schematic cross-sectional side view for illustrating an example of a reformer according to the present invention;
    • Figure 3 is a schematic cross-sectional side view for illustrating another example of the reformer according to the present invention;
    • Figure 4 is a schematic cross-sectional side view for illustrating a further example of the reformer according to the present invention; and
    • Figure 5 is a schematic cross-sectional side view for illustrating another example of the indirect internal reforming high temperature fuel cell according to the present invention.
    Description of Symbols
    • 1: reformer
    • 2: reforming vessel
    • 3: first partition plate
    • 4: second partition plate
    • 5: reforming catalyst bed
    • 6: SOFC
    • 7: module container
    • 8: electric heater
    Best Mode for Carrying Out the Invention
  • In the following, embodiments of the present invention will be described with reference to the drawings. However, the present invention is not limited by the embodiments described below.
  • Figure 1 is a schematic cross-sectional side view of an indirect internal reforming SOFC, which is an example of an indirect internal reforming high temperature fuel cell according to the present invention. This drawing shows a cross section perpendicular to the direction of flow of a gas in a reformer (the direction of flow of a reformed gas). In the drawing, the reformed gas flows in the direction perpendicular to the sheet of the drawing. The indirect internal reforming SOFC has a reformer 1 that produces a hydrogen-containing gas (reformed gas) from a hydrocarbon-based fuel using a steam reforming reaction and an SOFC 6 that generates electric power using the hydrogen-containing gas. That is, the hydrogen-containing gas (reformed gas) produced by the reformer 1 is supplied to an anode of the SOFC 6, an oxygen-containing gas, such as air, is supplied to a cathode of the SOFC 6, and the SOFC generates electric power by an electrochemical reaction between hydrogen and oxygen.
  • The indirect internal reforming SOFC further has a housing 7 (sometimes referred to as a module container hereinafter) that houses the reformer and the SOFC. That is, the reformer and the SOFC are modularized.
  • The reformer 1 has a reactor vessel (referred to also as a reforming vessel hereinafter) 2 and a reforming catalyst bed 5 packed with a granular catalyst housed in the reactor vessel 2. The reforming catalyst has steam reforming activity.
  • The reformer 1 is disposed at a position where the reformer 1 receives thermal radiation from the SOFC 6.
  • Here, the reformer has the shape of a rectangular parallelepiped. The SOFC also has the shape of a rectangular parallelepiped.
  • The reformer is disposed above the SOFC. At least in rated operation, the reforming vessel is heated at the lower surface by radiation heat from the SOFC. As an anode off gas (gas discharged from the anode) is burned on the upper surface of the SOFC, the reforming vessel is heated at the lower surface also by the combustion heat.
  • The reformer has a partition plate 3 that divides the reforming catalyst bed into at least two sections. The partition plate 3 extends in the reforming vessel from a part which is at a higher temperature in rated operation to a part which is at a lower temperature in rated operation. In the following, the partition plate will be sometimes referred to as a first partition plate.
  • Here, two planar partition plates 3 extend in the vertical direction. That is, the partition plates 3 extend from the surface (the lower surface) of the reforming vessel 2 facing the SOFC to the upper surface of the reforming vessel 2, the upper surface being located farther from the SOFC than the lower surface.
  • Thus, heat is transferred from the lower surface of the reactor vessel toward the upper surface through the partition plates 3, and the reforming catalyst in the upper part is also adequately heated.
  • In Figure 1, one planar partition plate 4 extending in the horizontal direction is provided in addition to the first partition plates. The partition plate 4 is preferably used to provide a uniform heat distribution in lateral direction. In the following, this partition plate will be sometimes referred to as a second partition plate.
  • The partition plates 3 and the partition plate 4 divide the reforming catalyst bed into six sections in total in the plane perpendicular to the direction of flow of the reforming gas.
  • [Partition Plate]
  • The first partition plate has a thermal conductivity higher than the effective thermal conductivity of the reforming catalyst bed. In case that the second partition plate is also provided, a thermal conductivity thereof is higher than the effective thermal conductivity of the reforming catalyst bed.
  • The effective thermal conductivity of the catalyst bed is an apparent thermal conductivity on the assumption that the catalyst bed is homogeneous and can be measured or calculated by an appropriate method.
  • The partition plates may be made of any appropriate material that is resistant to use environment and has a thermal conductivity higher than the effective thermal conductivity of the catalyst bed, such as stainless steel. In view of preventing deformation or destruction due to a difference in linear expansion coefficients, or when there is a possibility of embrittlement in a contact or joint part due to a chemical reaction, the partition plates are preferably made of the same material as the reactor vessel. For example, when the reactor vessel of the reformer is formed of metal plates, and the metal plates have a thermal conductivity higher than the effective thermal conductivity of the catalyst bed, the first and second partition plates are preferably made of the same metal as the reforming vessel.
  • The shape of the partition plates is not limited to the planar shape but may be any appropriate shape, such as a shape of a bent plate.
  • In Figure 1, two first partition plates 3 are disposed at regular intervals to trisect the reforming catalyst bed in the horizontal direction. However, the present invention is not limited to this configuration. It is essential only that the first partition plate(s) extends in the reforming vessel from a part heated to a higher temperature in rated operation toward a part heated to a lower temperature in rated operation. As a result, the partition plate(s) extends from a part closer to the heat source to a part farther from the heat source.
  • Each of Figures 2, 3 and 4 shows an example of a reformer that can replace the reformer shown in Figure 1. These drawings are also schematic cross-sectional views taken perpendicularly to the direction of flow of the gas in the reformer. In Figure 2, first partition plates 3 are disposed at higher densities in areas closer to the center (in the horizontal direction) of the reformer and at lower densities in areas farther from the center. In Figure 3, first partition plates 3 are disposed to radially extend from the center of the lower surface of the reformer vessel. In Figure 4, first partition plates 3 in the shape of a curved surface are disposed to radially extend from the center of the lower surface of the reformer vessel. Depending on the positional relationship with the heat source or the like, an appropriate one of the configurations shown in Figures 2, 3 and 4 may be selected.
  • Of course, the first partition plate is disposed not to inhibit the flow of the gas in the reformer. For example, the first partition plate may be disposed to extend along the direction of flow of the gas in the reformer (direction of flow of the reformed gas). The same holds true for the second partition plate.
  • In the configuration shown in Figure 1, the SOFC 6 heats the reactor vessel 2 from outside of the reactor vessel 2. However, the present invention is not limited to this configuration. Even if the reformer is provided with any other heat source than the fuel cell and the reactor vessel is heated from outside by the heat source, the first partition plates provide the same effect. For example, the reformer may have combusting means, such as a burner and a catalyst combustor, and the reforming vessel may be heated from outside by the combusting means. Or, the reformer may have heating means, such as an electric heater, provided outside the reactor vessel, and the reforming vessel may be heated from outside by the heating means.
  • Further, the reformer may be equipped with a heat source that heats the catalyst bed inside the reactor vessel. Figure 5 shows an indirect internal reforming high temperature fuel cell in which a reformer 1 has a heating means, such as an electric heater 8, inside a reactor vessel 2, and a catalyst bed is heated inside the reactor vessel 2 by the heating means. Also in this case, the first partition plates provide the same effect.
  • The reformer according to the present invention has a partition plate made of a material, such as metal, having a thermal conductivity higher than the effective thermal conductivity of the catalyst bed. The partition plate extends in the reactor vessel from a part which is at a higher temperature in rated operation to a part which is at a lower temperature in rated operation. Therefore, the thermal radiation from the high temperature fuel cell can be efficiently conducted to the entire catalyst bed, the catalyst bed can be more uniformly heated to a higher temperature, and the size of the reformer can be reduced.
  • [Hydrocarbon-based Fuel]
  • It is possible to use, as appropriate, a hydrocarbon-based fuel selected from among compounds of which molecules contain carbon and hydrogen (may also contain other elements such as oxygen) or mixtures thereof that are well known as a feedstock for reformed gas in the field of the high temperature fuel cell. It is possible to use compounds of which molecules contain carbon and hydrogen, such as hydrocarbons and alcohols. For example, hydrocarbon fuels such as methane, ethane, propane, butane, natural gas, liquefied petroleum gas (LPG), city gas, gasoline, naphtha, kerosene and gas oil, alcohols such as methanol and ethanol, and ethers such as dimethyl ether may be used.
  • Among others, kerosene and LPG are preferred because they are readily available. In addition, kerosene and LPG can be stored in a stand-alone manner and therefore are useful in areas where the city gas pipeline is not built. In addition, high temperature fuel cells using kerosene or LPG are useful as an emergency power supply. Kerosene is particularly preferred because it is easy to handle.
  • [High Temperature Fuel Cell]
  • The present invention may be suitably applied to an indirect internal reforming fuel cell in which a reformer can be heated by thermal radiation from a high temperature fuel cell. In addition to the SOFC, a molten carbonate fuel cell (MCFC) is an example of the high temperature fuel cell of this type.
  • The SOFC may be selected, as appropriate, from well-known SOFCs having various shapes, such as planar SOFCs and tubular SOFCs. The SOFC may have an appropriate shape, such as a rectangular parallelepiped stack of planar SOFCs (including a cubic stack of planar SOFCs), a cylindrical SOFC stack, a bundle of tubular SOFC cells, and a cylindrical tubular SOFC cells. Typical electrolytes used in the SOFC include oxygen-ion conductive ceramic and proton-ion conductive ceramic.
  • The MCFC may also be appropriately selected from among well-known MCFCs.
  • The SOFC and MCFC may be a single cell. However, in practice, a stack or bundle in which a plurality of single cells is arrayed is preferably used. In that case, the number of stacks or bundles can be one or more.
  • [Reformer]
  • The reformer has a reforming catalyst bed packed with a granular catalyst having steam reforming activity in a reactor vessel. The reforming catalyst having steam reforming activity may be selected, as appropriate, from among steam reforming catalysts which have steam reforming activity and autothermal reforming catalysts which have both of partial oxidation reforming activity and steam reforming activity.
  • The hydrocarbon-based fuel (vaporized beforehand as required) and steam and if necessary an oxygen-containing gas, such as air, may be supplied each independently or mixed beforehand to the reformer (reforming catalyst bed). The reforming gas is supplied to the anode of the high temperature fuel cell.
  • Among other indirect internal reforming high temperature fuel cells, the indirect internal reforming SOFC is superior in thermal efficiency. The indirect internal reforming SOFC has a reformer that produces a reforming gas containing hydrogen from a hydrocarbon-based fuel by a steam reforming reaction and a SOFC. The reformer may perform a steam reforming reaction or perform autothermal reforming in which the steam reforming reaction is accompanied with the partial oxidation reaction. From the viewpoint of power generation efficiency of the SOFC, it is preferred that no partial oxidation reaction occurs. Thus, the autothermal reforming is designed so that the steam reforming is predominant, and therefore, the overall reforming reaction is endothermic. The heat required for the reforming reaction is supplied from the SOFC. The reformer and the SOFC are housed in one module container and modularized. The reformer is disposed at a position where the reformer receives the thermal radiation from the SOFC. This arrangement allows the reformer to be heated by the thermal radiation from the SOFC during electric power generation. In addition, the anode off gas discharged from the SOFC may be burned at the outlet of the cell to heat the
  • SOFC.
  • In the indirect internal reforming SOFC, the reformer is preferably disposed at a position where direct radiation heat transfer from the SOFC to the outer surface of the reformer is possible. Therefore, it is preferred that there is substantially no obstacle between the reformer and the SOFC, or in other words, it is preferred to make the region between the reformer and the SOFC be an empty space. In addition, the distance between the reformer and the SOFC is preferably as short as possible.
  • Each supply gas is appropriately heated as required before being supplied to the reformer or the SOFC.
  • The module container may be any appropriate container capable of housing the SOFC and the reformer. The module container may be made of any appropriate material having resistance to the environment in which the module container is used, such as stainless steel. Connection ports are provided for the module container for gas interfacing or the like as required.
  • In particular, if the cell outlet opens in the module container, the module container is preferably hermetic in order to prevent communication between the interior of the module container and the surroundings (atmosphere).
  • [Reforming Catalyst]
  • Both the steam reforming catalyst and the autothermal reforming catalyst used in the reformer may be a well-known catalyst. Examples of the steam reforming catalyst include a ruthenium-based catalyst or a nickel-based catalyst, and examples of the autothermal reforming catalyst include a rhodium-based catalyst.
  • According to the present invention, a granular catalyst is used. For example, the granular catalyst may be a catalyst formed by performing tablet compression, pulverization and then particle size selection within an appropriate range, a catalyst formed by extrusion molding, a catalyst formed by mixing with an appropriate binder and extrusion molding, or a powdered catalyst. Alternatively, the catalyst may be a metal supported by a carrier formed by performing tablet compression, pulverization and then particle size selection within an appropriate range, a carrier formed by extrusion molding, a powdered carrier, or a carrier molded into an appropriate shape, such as a sphere, a ring, a tablet, a cylinder and a flake.
  • In the following, conditions in rated operation of the reformer for each of the steam reforming, the autothermal reforming and the partial oxidation reforming will be described.
  • In the steam reforming, steam is added to the hydrocarbon-based fuel, such as kerosene. For example, the reaction temperature of the steam reforming may range from 400°C to 1000°C, preferably from 500°C to 850°C, or more preferably from 550°C to 800°C. The amount of steam introduced into the reaction system is defined as a ratio (steam/carbon ratio) of the number of moles of water molecules to the number of moles of carbon atoms contained in the hydrocarbon-based fuel, and the value of the ratio preferably falls within a range of 1 to 10, more preferably within a range of 1.5 to 7, or further preferably within a range of 2 to 5. In the case where the hydrocarbon-based fuel is liquid, the space velocity (LHSV) is expressed as A/B, where A represents the flow rate (L/h) of the hydrocarbon-based fuel in the liquid state, and B represents the volume (L) of the catalyst bed. The value of the LHSV is preferably set within a range of 0.05 to 20 h-1, more preferably within a range of 0.1 to 10 h-1, or further preferably within a range of 0.2 to 5 h-1.
  • In the autothermal reforming, not only steam but also an oxygen-containing gas is added to the hydrocarbon-based fuel. The oxygen-containing gas is preferably air because air is readily available, although the oxygen-containing gas may be pure oxygen. The oxygen-containing gas may be added in order to balance the endothermic reaction involved with the steam reforming reaction and to obtain an amount of heat generation enough to keep or raise the temperature of the reforming catalyst bed and the SOFC. The amount of oxygen-containing gas added is, as a ratio (oxygen/carbon ratio) of the number of moles of oxygen molecules to the number of moles of carbon atoms contained in the hydrocarbon-based fuel, preferably within a range of 0.005 to 1, more preferably within a range of 0.01 to 0.75, or further preferably within a range of 0.02 to 0.6. For example, the reaction temperature of the autothermal reforming reaction is set within a range of 400°C to 1000°C, preferably within a range of 450°C to 850°C, or more preferably within a range of 500°C to 800°C. In the case where the hydrocarbon-based fuel is liquid, the space velocity (LHSV) is preferably selected within a range of 0.05 to 20, more preferably within a range of 0.1 to 10, or further preferably within a range of 0.2 to 5. The amount of steam introduced into the reaction system is, as the steam/carbon ratio, preferably within a range of 1 to 10, more preferably within a range of 1.5 to 7, or further preferably within a range of 2 to 5.
  • [Other Devices]
  • As required, the indirect internal reforming high temperature fuel cell according to the present invention may be additionally provided with a well-known component of a high temperature fuel cell system, as appropriate. For example, such a component may be a desulfurizer that reduces the sulfur content of the hydrocarbon-based fuel; a vaporizer that vaporizes a liquid; pressure increasing means that pressurizes various kinds of fluids, such as a pump, a compressor and a blower; flow rate controlling means or flow path blocking/switching means that regulates the flow rate of a fluid or blocks a fluid flow or switches among fluid flow paths, such as a valve; a heat exchanger that performs heat exchange or heat recovery; a condenser that condenses a gas; heating/warming means that externally heats various kinds of equipment using steam or the like; storage means that stores the hydrocarbon-based fuel or a combustible material; an air or electric system for instrumentation; a signal system for control; a control device; and an electric system for output or powering.
  • Industrial Applicability
  • The reformer and the indirect internal reforming high temperature fuel cell according to the present invention can be applied to, for example, a stationary or mobile power generating system or in a cogeneration system.

Claims (3)

  1. An indirect internal reforming high temperature fuel cell, comprising:
    a reformer for producing a hydrogen-containing gas from a hydrocarbon-based fuel by a steam reforming reaction; and
    a high temperature fuel cell that generates electric power using the hydrogen-containing gas,
    the reformer comprising a reactor vessel and a reforming catalyst bed packed with a granular catalyst having steam reforming activity in the reactor vessel, and
    the reformer being disposed at a position where the reformer receives thermal radiation from the high temperature fuel cell,
    wherein the reformer has a partition plate for dividing the reforming catalyst bed into at least two sections,
    a thermal conductivity of the partition plate is higher than an effective thermal conductivity of the catalyst bed, and
    the partition plate extends in the reactor vessel from a part which is at a higher temperature in rated operation to a part which is at a lower temperature in rated operation,
    the high temperature fuel cell is essentially in a shape of rectangular parallelepiped, and is configured so that an anode off gas is able to be burned on the upper surface of the high temperature fuel cell,
    the reformer is disposed above the high temperature fuel cell, and is configured so that a flow direction of gas in the reformer is essentially horizontal.
  2. The indirect internal reforming high temperature fuel cell according to claim 1, wherein the reformer is essentially in a shape of a rectangular parallelepiped.
  3. The indirect internal reforming high temperature fuel cell according to claim 1 or 2, wherein the reformer further comprises a second partition plate extending horizontally.
EP08752801.4A 2007-05-16 2008-05-15 Reformer and indirect internal reforming-type high-temperature fuel cell Not-in-force EP2157048B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007130486A JP5095264B2 (en) 2007-05-16 2007-05-16 Reformer and indirect internal reforming type high temperature fuel cell
PCT/JP2008/058943 WO2008140116A1 (en) 2007-05-16 2008-05-15 Reformer and indirect internal reforming-type high-temperature fuel cell

Publications (3)

Publication Number Publication Date
EP2157048A1 EP2157048A1 (en) 2010-02-24
EP2157048A4 EP2157048A4 (en) 2012-11-07
EP2157048B1 true EP2157048B1 (en) 2014-01-08

Family

ID=40002303

Family Applications (1)

Application Number Title Priority Date Filing Date
EP08752801.4A Not-in-force EP2157048B1 (en) 2007-05-16 2008-05-15 Reformer and indirect internal reforming-type high-temperature fuel cell

Country Status (8)

Country Link
US (1) US8338041B2 (en)
EP (1) EP2157048B1 (en)
JP (1) JP5095264B2 (en)
KR (1) KR101422316B1 (en)
CN (1) CN101679029B (en)
CA (1) CA2687231A1 (en)
TW (1) TWI416790B (en)
WO (1) WO2008140116A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101228631B1 (en) 2010-12-03 2013-01-31 재단법인 포항산업과학연구원 Reforming apparatus
JP6550813B2 (en) * 2015-03-18 2019-07-31 富士電機株式会社 Fuel cell module
JP6495767B2 (en) * 2015-07-03 2019-04-03 日立造船株式会社 Fuel cell system
DE112017005356T5 (en) * 2016-10-24 2019-07-11 Precision Combustion, Inc. Solid oxide cell with internal heating device
JP7240870B2 (en) * 2018-12-20 2023-03-16 三菱重工業株式会社 Combustion burner housing device and dummy port closing method

Family Cites Families (32)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61190867A (en) * 1985-02-19 1986-08-25 Toshiba Corp Fuel cell power generating system
JPH02102101A (en) * 1988-10-12 1990-04-13 Fuji Electric Co Ltd Reformer for fuel cell
JPH04265147A (en) * 1991-02-19 1992-09-21 Fuji Electric Co Ltd Fuel reformer
JPH05129026A (en) 1991-11-07 1993-05-25 Sanyo Electric Co Ltd Internal reforming type fuel cell
JPH09503615A (en) 1993-10-06 1997-04-08 セラマテック,インコーポレーテッド Built-in converter / CPN solid oxide fuel cell stack / module design
JPH07272741A (en) * 1994-03-31 1995-10-20 Mitsubishi Heavy Ind Ltd Module structure for cylindrical solid electrolytic fuel cell
JPH0930801A (en) * 1995-07-19 1997-02-04 Mitsubishi Electric Corp Reformation reactor
JPH1017303A (en) * 1996-06-28 1998-01-20 Daikin Ind Ltd Reformer for fuel cell
JPH1111901A (en) * 1997-06-24 1999-01-19 Fuji Electric Co Ltd Reforming device for fuel cell power generation unit
KR20010075696A (en) 1999-09-10 2001-08-09 이노우에 노리유끼 Apparatus for producing hydrogen gas and fuel cell system using the same
JP2001151502A (en) * 1999-11-26 2001-06-05 Daikin Ind Ltd Fuel reforming device
JP4644892B2 (en) * 1999-12-16 2011-03-09 ダイキン工業株式会社 Reformer
CN1219694C (en) * 1999-12-28 2005-09-21 大金工业株式会社 Partical oxidizing modifying device
DE10001064B4 (en) * 2000-01-13 2004-03-11 Ballard Power Systems Ag Reforming reactor in layered construction
CA2357960C (en) * 2000-10-10 2007-01-30 Tokyo Gas Co., Ltd. Single-pipe cylinder type reformer
JP2002151127A (en) * 2000-11-16 2002-05-24 Ngk Insulators Ltd Cogeneration power plant
JP3539562B2 (en) * 2001-05-31 2004-07-07 日本電信電話株式会社 Solid oxide fuel cell stack
DE10149060A1 (en) * 2001-10-05 2003-04-30 Daimler Chrysler Ag Process for reforming liquid hydrocarbon mixtures
AU2002350312A1 (en) * 2001-12-14 2003-06-30 Sgdl Systemes Inc. Method and apparatus for generating m-degree forms in a n-dimension space
JP2003226506A (en) * 2002-02-06 2003-08-12 Mitsubishi Electric Corp Reformer for fuel cell
JP4645876B2 (en) * 2002-04-26 2011-03-09 日産自動車株式会社 Solid oxide fuel cell
EP1408003A1 (en) * 2002-10-10 2004-04-14 Matsushita Electric Industrial Co., Ltd. Hydrogen generator and electric generator using the same
WO2004035469A1 (en) * 2002-10-17 2004-04-29 Toyo Radiator Co., Ltd. Autooxidation internal heating type steam reforming system
JP4369685B2 (en) 2003-02-25 2009-11-25 京セラ株式会社 Operation method of fuel cell
JP2004269332A (en) 2003-03-11 2004-09-30 Nissan Motor Co Ltd Fuel reformer
JP4789451B2 (en) * 2003-11-28 2011-10-12 京セラ株式会社 Fuel cell
WO2005073126A1 (en) * 2004-01-30 2005-08-11 Idemitsu Kosan Co., Ltd. Reformer
JP4906249B2 (en) * 2004-06-30 2012-03-28 京セラ株式会社 Fuel cell reformer
JP4555149B2 (en) * 2005-05-23 2010-09-29 本田技研工業株式会社 Fuel cell system and operation method thereof
JP2006327904A (en) 2005-05-30 2006-12-07 Babcock Hitachi Kk Hydrogen manufacturing apparatus and fuel cell system provided with the hydrogen manufacturing apparatus
JP2006351293A (en) * 2005-06-14 2006-12-28 Idemitsu Kosan Co Ltd Solid oxide fuel cell system
JP5058809B2 (en) * 2005-09-30 2012-10-24 パナソニック株式会社 Hydrogen generator and fuel cell system

Also Published As

Publication number Publication date
EP2157048A4 (en) 2012-11-07
US20100227235A1 (en) 2010-09-09
TWI416790B (en) 2013-11-21
JP2008285355A (en) 2008-11-27
CN101679029A (en) 2010-03-24
EP2157048A1 (en) 2010-02-24
KR101422316B1 (en) 2014-07-22
TW200919817A (en) 2009-05-01
CA2687231A1 (en) 2008-11-20
US8338041B2 (en) 2012-12-25
KR20100024934A (en) 2010-03-08
CN101679029B (en) 2013-06-12
WO2008140116A1 (en) 2008-11-20
JP5095264B2 (en) 2012-12-12

Similar Documents

Publication Publication Date Title
EP2173000A1 (en) Fuel battery system and its activating method
EP2278650B1 (en) Method for operating indirect internal reforming solid oxide fuel cell system
US8841039B2 (en) Indirect internal reforming solid oxide fuel cell system
JP2008287959A (en) Indirect internal reform type high-temperature type fuel cell
KR20100097197A (en) Fuel cell system and method for starting the same
KR101508803B1 (en) Fuel cell system and method of load following operation of the same
JP2009176660A (en) Shutdown method of indirect internal reforming solid oxide fuel cell
EP2157048B1 (en) Reformer and indirect internal reforming-type high-temperature fuel cell
JP2009059658A (en) Indirect interior-reformed solid oxide fuel cell
JP5078698B2 (en) Load following operation method of fuel cell system
EP2267827A1 (en) Fuel cell system and method of load following operation of the same
JP5078697B2 (en) Load following operation method of fuel cell system
JP2009059657A (en) Indirect interior-reformed solid oxide fuel cell
JP5463006B2 (en) Operation method of solid oxide fuel cell system
JP5007077B2 (en) Reformer and indirect internal reforming type solid oxide fuel cell
JP2008186759A (en) Indirect internal reforming solid oxide fuel cell system and method for operating indirect internal reforming solid oxide fuel cell
US8865358B2 (en) Method for load following operation of fuel cell system

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20091207

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: AL BA MK RS

DAX Request for extension of the european patent (deleted)
A4 Supplementary search report drawn up and despatched

Effective date: 20121010

RIC1 Information provided on ipc code assigned before grant

Ipc: H01M 8/12 20060101ALI20121002BHEP

Ipc: C01B 3/38 20060101AFI20121002BHEP

Ipc: H01M 8/06 20060101ALI20121002BHEP

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20130731

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MT NL NO PL PT RO SE SI SK TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: AT

Ref legal event code: REF

Ref document number: 648618

Country of ref document: AT

Kind code of ref document: T

Effective date: 20140215

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602008029783

Country of ref document: DE

Effective date: 20140220

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 648618

Country of ref document: AT

Kind code of ref document: T

Effective date: 20140108

REG Reference to a national code

Ref country code: NL

Ref legal event code: VDEP

Effective date: 20140108

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140408

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140508

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140508

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602008029783

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

26N No opposition filed

Effective date: 20141009

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140515

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: DE

Ref legal event code: R097

Ref document number: 602008029783

Country of ref document: DE

Effective date: 20141009

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20140531

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20140531

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20140515

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 9

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140409

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20080515

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140108

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 10

REG Reference to a national code

Ref country code: GB

Ref legal event code: 732E

Free format text: REGISTERED BETWEEN 20170511 AND 20170517

REG Reference to a national code

Ref country code: GB

Ref legal event code: 732E

Free format text: REGISTERED BETWEEN 20170518 AND 20170524

REG Reference to a national code

Ref country code: FR

Ref legal event code: CA

Effective date: 20170628

Ref country code: FR

Ref legal event code: CD

Owner name: JX NIPPON OIL & ENERGY CORPORATION, JP

Effective date: 20170628

REG Reference to a national code

Ref country code: DE

Ref legal event code: R082

Ref document number: 602008029783

Country of ref document: DE

Representative=s name: SCHWABE SANDMAIR MARX PATENTANWAELTE RECHTSANW, DE

Ref country code: DE

Ref legal event code: R081

Ref document number: 602008029783

Country of ref document: DE

Owner name: KYOCERA CORP., JP

Free format text: FORMER OWNER: JX NIPPON OIL & ENERGY CORP., TOKIO/TOKYO, JP

Ref country code: DE

Ref legal event code: R081

Ref document number: 602008029783

Country of ref document: DE

Owner name: KYOCERA CORP., JP

Free format text: FORMER OWNER: NIPPON OIL CORP., TOKIO/TOKYO, JP

Ref country code: DE

Ref legal event code: R081

Ref document number: 602008029783

Country of ref document: DE

Owner name: KYOCERA CORPORATION, KYOTO-SHI, JP

Free format text: FORMER OWNER: NIPPON OIL CORP., TOKIO/TOKYO, JP

Ref country code: DE

Ref legal event code: R081

Ref document number: 602008029783

Country of ref document: DE

Owner name: KYOCERA CORPORATION, KYOTO-SHI, JP

Free format text: FORMER OWNER: JX NIPPON OIL & ENERGY CORP., TOKIO/TOKYO, JP

Ref country code: DE

Ref legal event code: R082

Ref document number: 602008029783

Country of ref document: DE

Representative=s name: SSM SANDMAIR PATENTANWAELTE RECHTSANWALT PARTN, DE

REG Reference to a national code

Ref country code: FR

Ref legal event code: CA

Effective date: 20170628

Ref country code: FR

Ref legal event code: TP

Owner name: KYOCERA CORPORATION, JP

Effective date: 20170628

REG Reference to a national code

Ref country code: DE

Ref legal event code: R082

Ref document number: 602008029783

Country of ref document: DE

Representative=s name: SCHWABE SANDMAIR MARX PATENTANWAELTE RECHTSANW, DE

Ref country code: DE

Ref legal event code: R081

Ref document number: 602008029783

Country of ref document: DE

Owner name: KYOCERA CORPORATION, KYOTO-SHI, JP

Free format text: FORMER OWNER: KYOCERA CORP., KYOTO, JP

Ref country code: DE

Ref legal event code: R082

Ref document number: 602008029783

Country of ref document: DE

Representative=s name: SSM SANDMAIR PATENTANWAELTE RECHTSANWALT PARTN, DE

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20210420

Year of fee payment: 14

Ref country code: FR

Payment date: 20210412

Year of fee payment: 14

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20210422

Year of fee payment: 14

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602008029783

Country of ref document: DE

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20220515

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220531

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20220515

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20221201